About   Help   FAQ
Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Tg(Drd1-cre)EY262Gsat
transgene insertion EY262, GENSAT Project at Rockefeller University
MGI:3836631
Summary 5 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
cn1
Ehmt2tm1.1Tara/Ehmt2tm1.1Tara
Tg(Drd1-cre)EY262Gsat/0
involves: 129P2/OlaHsd * C57BL/6 * FVB/N MGI:4418568
cn2
Nlgn3tm4.1Sud/Y
Tg(Drd1-cre)EY262Gsat/0
involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * FVB/N * SJL MGI:5660864
cn3
Nlgn3tm1Sud/Y
Tg(Drd1-cre)EY262Gsat/0
involves: 129S1/Sv * 129X1/SvJ * FVB/N MGI:5660866
cn4
Mir128-2tm1.1Ans/Mir128-2tm1.1Ans
Tg(Drd1-cre)EY262Gsat/0
involves: BALB/cJ * C57BL/6J * FVB/N MGI:5563804
cn5
Ppp1r1btm5.1Pggd/Ppp1r1btm5.1Pggd
Tg(Drd1-cre)EY262Gsat/0
Tg(Drd1-EGFP)X60Gsat/0
involves: C57BL/6 * FVB/N * FVB/NTac MGI:4830459


Genotype
MGI:4418568
cn1
Allelic
Composition
Ehmt2tm1.1Tara/Ehmt2tm1.1Tara
Tg(Drd1-cre)EY262Gsat/0
Genetic
Background
involves: 129P2/OlaHsd * C57BL/6 * FVB/N
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Ehmt2tm1.1Tara mutation (0 available); any Ehmt2 mutation (57 available)
Tg(Drd1-cre)EY262Gsat mutation (2 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
behavior/neurological
• decrease in Drd-1 agonist SKE 81291 induced locomotor and exploratory responses
• decrease in Drd-1 agonist SKE 81291 induced locomotor and exploratory responses

nervous system
N
• no major impact on regulation of neuronal morphology and basal electrophysiological features of Drd2-expressing MSNs in the striatum




Genotype
MGI:5660864
cn2
Allelic
Composition
Nlgn3tm4.1Sud/Y
Tg(Drd1-cre)EY262Gsat/0
Genetic
Background
involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * FVB/N * SJL
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Nlgn3tm4.1Sud mutation (0 available); any Nlgn3 mutation (36 available)
Tg(Drd1-cre)EY262Gsat mutation (2 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
behavior/neurological
• mice exhibit increased learning rate on the accelerating rotarod
• mice exhibit increased open-field activity




Genotype
MGI:5660866
cn3
Allelic
Composition
Nlgn3tm1Sud/Y
Tg(Drd1-cre)EY262Gsat/0
Genetic
Background
involves: 129S1/Sv * 129X1/SvJ * FVB/N
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Nlgn3tm1Sud mutation (1 available); any Nlgn3 mutation (36 available)
Tg(Drd1-cre)EY262Gsat mutation (2 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
behavior/neurological
• mice exhibit increased learning rate but similar initial coordination on the accelerating rotarod
• mice perform similarly to wild-type littermates on the first trial of an accelerating rotarod, however in the last several trials, mice exhibit enhanced performance, with increased time on the rotarod before falling off compared to wild-type mice, indicating enhanced formation of repetitive motor routine




Genotype
MGI:5563804
cn4
Allelic
Composition
Mir128-2tm1.1Ans/Mir128-2tm1.1Ans
Tg(Drd1-cre)EY262Gsat/0
Genetic
Background
involves: BALB/cJ * C57BL/6J * FVB/N
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Mir128-2tm1.1Ans mutation (0 available); any Mir128-2 mutation (0 available)
Tg(Drd1-cre)EY262Gsat mutation (2 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• at about 5 months of age

behavior/neurological
• juvenile
• administration of a MAP2K1 specific inhibitor SL327 normalizes locomotor activity

nervous system
• about a 20% increase in functional dendritic spines in striatal slices
• enhanced dendritic excitability in striatal slices




Genotype
MGI:4830459
cn5
Allelic
Composition
Ppp1r1btm5.1Pggd/Ppp1r1btm5.1Pggd
Tg(Drd1-cre)EY262Gsat/0
Tg(Drd1-EGFP)X60Gsat/0
Genetic
Background
involves: C57BL/6 * FVB/N * FVB/NTac
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Ppp1r1btm5.1Pggd mutation (0 available); any Ppp1r1b mutation (18 available)
Tg(Drd1-cre)EY262Gsat mutation (2 available)
Tg(Drd1-EGFP)X60Gsat mutation (1 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
nervous system
• loss of expression in striatopallidal and striatonigral neurons results in a reduced LTP at the corticostriatal synapses

behavior/neurological
• haloperidol-induced catalepsy is reduced
• L-DOPA-induced dyskinesia. is absent
• in an open-field test





Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
Citing These Resources
Funding Information
Warranty Disclaimer, Privacy Notice, Licensing, & Copyright
Send questions and comments to User Support.
last database update
11/12/2024
MGI 6.24
The Jackson Laboratory